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微小RNA-429在体外抑制胃癌细胞的生长。

MiRNA-429 suppresses the growth of gastric cancer cells in vitro.

作者信息

Liu Di, Xia Peng, Diao Dongmei, Cheng Yao, Zhang Hao, Yuan Dawei, Huang Chen, Dang Chengxue

机构信息

Department of Surgical Oncology, the First Affiliated Hospital, Medical School of Xi'an Jiaotong University, Xi'an, Shaanxi 710061, China;

出版信息

J Biomed Res. 2012 Sep;26(5):389-93. doi: 10.7555/JBR.26.20120029. Epub 2012 Sep 20.

Abstract

Micro-RNAs (miRNAs) have been found to be implicated in a very wide range of physiological processes. This study was aimed to investigate the regulation of miRNA-429 (miR-429) in gastric cancer cells on cell proliferation and apoptosis. Quantitative PCR was employed to detect the expressions of miR-429 after eukaryotic expression plasmid of miR-429 and its inhibitor were transiently transfected into poorly differentiated human gastric cancer cell line BGC823. The 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) reduction assays were used to examine proliferation ability. Apoptosis was analyzed by flow cytometry after transfection. The results showed that 48 h after transfection, overexpression of miR-429 reached maximum efficiency. Compared with mock transfection, miR-429 inhibited tumor cell proliferation significantly (P < 0.05) at 48 h and 72 h. of Overexpression of miR-429 promoted tumor cell apoptosis when compared with mock transfected cells (P < 0.05). On the contrary, miR-429 inhibitor promoted tumor cell proliferation and inhibited apoptosis when compared with controls (P < 0.05). Our results suggested that miRNA-429 may serve as a tumor suppressor during tumorigenesis of gastric cancer and may be a potential gastric cancer therapeutic target.

摘要

微小RNA(miRNA)已被发现与非常广泛的生理过程有关。本研究旨在探讨胃癌细胞中miRNA - 429(miR - 429)对细胞增殖和凋亡的调控作用。将miR - 429及其抑制剂的真核表达质粒瞬时转染入低分化人胃癌细胞系BGC823后,采用定量PCR检测miR - 429的表达。采用3 -(4,5 - 二甲基噻唑 - 2 - 基)- 2,5 - 二苯基四氮唑溴盐(MTT)还原试验检测增殖能力。转染后通过流式细胞术分析细胞凋亡情况。结果显示,转染后48小时,miR - 429的过表达达到最大效率。与空载体转染相比,miR - 429在48小时和72小时时显著抑制肿瘤细胞增殖(P < 0.05)。与空载体转染细胞相比,miR - 429过表达促进肿瘤细胞凋亡(P < 0.05)。相反,与对照组相比,miR - 429抑制剂促进肿瘤细胞增殖并抑制凋亡(P < 0.05)。我们的结果表明,miRNA - 429在胃癌发生过程中可能作为一种肿瘤抑制因子,可能是潜在的胃癌治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/209c/3597780/7031d19ff997/jbr-26-05-389-g001.jpg

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